FDA.reportPublic FDA data

NDC 67877-433-33 - Aripiprazole

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
67877-433
Requested NDC
67877-433-33
Package NDCs from labels
67877-433-03, 67877-433-01, 67877-433-05, 67877-433-33, 67877-433-38, 67877-433-32
Manufacturer
REMEDYREPACK INC.
Effective date
2026-07-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Aripiprazole - REMEDYREPACK INC.REMEDYREPACK INC.2026-07-30HUMAN PRESCRIPTION DRUG LABEL
Aripiprazole - Coupler LLCCoupler LLC2026-07-06HUMAN PRESCRIPTION DRUG LABEL
Aripiprazole - Bryant Ranch PrepackBryant Ranch Prepack2026-01-28HUMAN PRESCRIPTION DRUG LABEL
Aripiprazole - Ascend Laboratories, LLC | Alkem Laboratories LimitedAscend Laboratories, LLC | Alkem Laboratories Limited2025-10-01Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67877-433-01Aripiprazole100 in 1 BOTTLETABLET10026
67877-433-03Aripiprazole30 in 1 BOTTLETABLET3026
67877-433-05Aripiprazole500 in 1 BOTTLETABLET50026
67877-433-32Aripiprazole1 in 1 CARTONTABLET126
67877-433-32Aripiprazole7 in 1 BLISTER PACKTABLET726
67877-433-33Aripiprazole10 in 1 BLISTER PACKTABLET1026
67877-433-38Aripiprazole10 in 1 CARTONTABLET1026

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67877-433ARIPIPRAZOLE TABLET [ASCEND LABORATORIES, LLC]24Current NDC, Legacy NDC, 7 package rows20240229_c7040fef-96a7-4429-9a8e-ec3ab17a8019.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67877-433-01EA - Each67877-433bd47d6d0-84af-4087-aca8-c184b2e501e312019-08-06
67877-433-03EA - Each67877-43362f42f38-aa2a-47ea-ba33-9f69c11ba69312019-08-06
67877-433-05EA - Each67877-4335d426b23-cd0e-49cd-a1fe-b1adda85487712020-07-13

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 5 of 10 · 183 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Calamine Plus Pramoxine HClCALAMINE PLUS SPRAYHY-VEE, INC415ecfe9-3145-f23e-e063-6394a90adfd82025-11-17WarningsExact identifier
unii: 1K09F3G675
Au Kah Chuen FugicalCALAMINE AND DIPHENHYDRAMINE HYDROCHLORIDZhejiang Dingtai Pharmaceutical Co., Ltd5b4add17-6c3d-4093-826a-2edb41c1d1db2025-11-10WarningsExact identifier
unii: 1K09F3G675
FARGELIN HEMORRHOIDALCALAMINE, PETROLATUM AND PHENYLEPHRINE HYDROCHLORIDEMADISON ONE ACME INC6844ad63-512d-496a-9458-011894185b0d2025-11-10WarningsExact identifier
unii: 1K09F3G675
Calamine PlusCALAMINE PLUS PRAMOXINE HCLChain Drug Marketing Association Inc1a3f8819-58cf-8923-e063-6394a90a37af2025-11-06WarningsExact identifier
unii: 1K09F3G675
Calamine Plus Pramoxine HClCALAMINE PLUS NO TOUCH SPRAYPremier Brands of America Inc.36481d67-2346-470b-e063-6294a90aae992025-11-03WarningsExact identifier
unii: 1K09F3G675
Calamine PlusCALAMINE PLUS PRAMOXINE HCLAmerisourceBergen Drug Corporationf161e151-4fab-2fbc-e053-2a95a90a54372025-10-30WarningsExact identifier
unii: 1K09F3G675
REMEDY Calazime Skin ProtectantCALAMINE, MENTHOL, WHITE PETROLATUM, ZINC OXIDEMedline Industries, LP1295cfcc-5b61-481b-964b-f53ffd0cb58e2025-10-30WarningsExact identifier
unii: 1K09F3G675
Calamine PlusCALAMINE PLUS PRAMOXINE HCLMeijer Distribution Inc.03c46823-0b1f-4101-e063-6294a90aaf942025-10-30WarningsExact identifier
unii: 1K09F3G675
Aveeno Anti-Itch ConcentratedZINC OXIDE, FERRIC OXIDE RED, AND PRAMOXINE HYDROCHLORIDEKenvue Brands LLC07f4d4d0-9cee-46c3-bc71-2024abd31c9e2025-10-29WarningsExact identifier
unii: 1K09F3G675
Calamine Plus Pramoxine HClCALAMINE PLUS SPRAYPremier Brands of America, Inc.d3452573-f91f-f157-e053-2a95a90a1ad82025-10-27WarningsExact identifier
unii: 1K09F3G675
AripiprazoleARIPIPRAZOLEDr.Reddys Laboratories Inc178f09f0-e08e-452b-b817-717c5c49e1102025-10-24Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 349547
rxcui: 349553
rxcui: 602964
rxcui: 349545
rxcui: 349490
rxcui: 402131
unii: 82VFR53I78
AripiprazoleARIPIPRAZOLENuCare Pharmaceuticals, Inc.414b7fd2-6a63-af39-e063-6394a90a00b82025-10-16Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 349545
unii: 82VFR53I78
AripiprazoleARIPIPRAZOLEPD-Rx Pharmaceuticals, Inc.0cf6655e-d59a-4ebd-9698-195cad2adbd52025-10-14Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 402131
unii: 82VFR53I78
AripiprazoleARIPIPRAZOLEAjanta Pharma USA Inc.d0f910b5-adef-4a93-9369-70f1ed5415032025-10-10Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 349547
rxcui: 349553
rxcui: 602964
rxcui: 349545
rxcui: 349490
rxcui: 402131
unii: 82VFR53I78
ARIPIPRAZOLEARIPIPRAZOLEAccord Healthcare, Inc.85cc7d25-414b-4b6f-a03a-48af908a16a12025-10-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 349547
rxcui: 349553
rxcui: 602964
rxcui: 349545
rxcui: 349490
rxcui: 402131
unii: 82VFR53I78
AripiprazoleARIPIPRAZOLEAscend Laboratories, LLCc7040fef-96a7-4429-9a8e-ec3ab17a80192025-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA207105
ndc (package): 67877-435-33
ndc (package): 67877-430-05
ndc (package): 67877-432-38
ndc (package): 67877-434-05
ndc (package): 67877-433-05
ndc (package): 67877-430-01
ndc (package): 67877-434-33
ndc (package): 67877-430-32
ndc (package): 67877-431-32
ndc (package): 67877-434-03
ndc (package): 67877-432-33
ndc (package): 67877-433-03
ndc (package): 67877-432-05
ndc (package): 67877-431-38
ndc (package): 67877-431-01
ndc (package): 67877-435-01
ndc (package): 67877-430-03
ndc (package): 67877-434-01
ndc (package): 67877-434-38
ndc (package): 67877-430-33
ndc (package): 67877-432-01
ndc (package): 67877-432-32
ndc (package): 67877-432-03
ndc (package): 67877-433-32
ndc (package): 67877-431-05
ndc (package): 67877-433-38
ndc (package): 67877-435-03
ndc (package): 67877-431-33
ndc (package): 67877-430-38
ndc (package): 67877-431-03
ndc (package): 67877-435-05
ndc (package): 67877-433-33
ndc (package): 67877-433-01
ndc (package): 67877-435-38
ndc (product): 67877-434
ndc (product): 67877-435
ndc (product): 67877-432
ndc (product): 67877-431
ndc (product): 67877-433
ndc (product): 67877-430
ndc11 (package): 67877043333
rxcui: 349547
rxcui: 349553
rxcui: 602964
rxcui: 349545
rxcui: 349490
rxcui: 402131
spl id: 583fc581-09d7-4d4f-a079-08ba9d00f775
spl set id: c7040fef-96a7-4429-9a8e-ec3ab17a8019
unii: 82VFR53I78
PowderTITANIUM DIOXIDEOxygen Development LLC08b52f29-c1a0-c673-e063-6294a90a9a7a2025-09-05WarningsExact identifier
unii: 1K09F3G675
PowderTITANIUM DIOXIDEOxygen Development LLC08b8003f-40be-3380-e063-6294a90a4f6b2025-09-05WarningsExact identifier
unii: 1K09F3G675
AripiprazoleARIPIPRAZOLEAvPAK7df4c83e-13d8-25b1-57eb-08d26ba035652025-08-26Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 349547
rxcui: 349553
rxcui: 602964
rxcui: 349545
rxcui: 349490
rxcui: 402131
unii: 82VFR53I78
AripiprazoleARIPIPRAZOLENuCare Pharmaceuticals, Inc.3cf72cc6-ae43-bfd5-e063-6294a90a18b02025-08-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 402131
unii: 82VFR53I78

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.